RecruitingPhase 4NCT06476210
The Safety and Efficacy of BDL(Bedaquiline Plus Delamanid Plus Linezolid) Regimen in Subjects With Pulmonary Infection of Multi-drug Resistant Tuberculosis (MDR-TB) or Rifampicin-Resistant Tuberculosis (RR-TB)
Studying Primary pulmonary tuberculosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Beijing Chest Hospital
- Principal Investigator
- Yuhong Liu, Ph.DBeijing Chest Hostal
- Intervention
- BDL regimen(drug)
- Enrollment
- 45 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2026
Study locations (7)
- Anhui Chest Hospital, Hefei, Anhui, China
- Beijing Chest Hospital, Beijing, Beijing Municipality, China
- Wuhan Institute for Tuberculosis Control, Wuhan, Hubei, China
- Changsha Central Hospital, Changsha, Hunan, China
- Hunan Chest Hospital, Changsha, Hunan, China
- Shandong Public Health Clinical Center, Jinan, Shandong, China
- Public Health Clinical Meadical Center of Chengdu, Chengdu, Sichuan, China
Collaborators
Public Health Clinical Medical Center of Chengdu · Wuhan Institute for Tuberculosis Control · Changsha Central Hospital · Anhui Chest Hospital · Hunan Chest Hospital · Shandong Public Health Clinical Center
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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